Introduction
Monoclonal antibodies blocking the cytotoxic T lymphocyte associated antigen 4 (CTLA4), a key negative regulator of the immune system, induce regression of tumors in mice and humans, and are being pursued as treatment for cancer [
1‐
4]. CTLA4 blocking antibodies break tolerance to self tissues, as clearly demonstrated by the autoimmune phenomena in CTLA4 knock out mice [
5,
6], which results in autoimmune toxicities in patients. Understanding the immunological mechanisms guiding antitumor responses and anti-self toxicities may allow improving the use of this class of agents in the clinic.
The emerging clinical data suggests that a minority of patients with metastatic melanoma (in the range of 10%) achieve durable objective tumor responses when treated with CTLA4 blocking monoclonal antibodies, with most being relapse-free up to 7 years later. However, a significant proportion of patients (in the range of 20–30%) develop clinically-relevant toxicities, most often autoimmune or inflammatory in nature [
2‐
4]. There is a prevalent thought that toxicity and response are correlated after therapy with anti-CTLA4 blocking monoclonal antibodies. This conclusion is based mainly on statistical correlations in 2 × 2 tables grouping patients with toxicities and/or objective responses. However, even though patients with a response are more likely to have toxicities in these series, most patients with toxicity do not have a tumor response and there are occasional patients with an objective tumor response who never developed clinically-relevant toxicities [
2,
7], thereby suggesting to us that the relationship between toxicity and response is not linear. If we assume that both phenomena (toxicity and response) are mediated by activation of lymphocytes, then we need to question their antigen specificity, since it is unlikely that the same T cells that mediate toxicity in the gut, for example, will be responsible for antitumor activity against melanoma. It is more likely that the same threshold of CTLA4 blockade may lead to activation of lymphocytes reactive to self-tissues and cancer. Therefore, we studied a differentiated subset of cells termed Th17, which have emerged as key mediators of autoimmunity and inflammation for their potential implication in toxicity and responses after anti-CTLA4 therapy.
The description of Th17 cells has substantially advanced our understanding of T cell-mediated inflammation and immunity [
8]. These cells are characterized as preferential producers of IL-17A (also known as IL-17), IL-17F, IL-21, IL-22, and IL-26 in humans. The production of IL-17 is used to identify Th17 cells and differentiate them from IFN-γ-producing Th1 cells, or IL-4-producing Th2 cells. The transcription factor retinoic-acid-related orphan receptor-γτ (ROR-γτ) and IL-1β and IL-23 are important for the generation of human Th17 cells
in vitro and
in vivo [
8,
9]. Th17 cells are potent inducers of tissue inflammation, and dysregulated expression of IL-17 appears to initiate organ-specific autoimmunity; this has been best characterized in mouse models of colitis [
10], experimental autoimmune encephalomyelitis (EAE) [
11,
12], rheumatoid arthritis [
13] and autoimmune myocarditis [
14]. In these models, mice treated with anti-IL-17 antibodies have lower incidence of disease, slower progression of disease and reduced scores of disease severity. Treatment with anti-IL-17 antibodies nine days after inducing EAE significantly delayed the onset of paralysis. When the treatment was started at the peak of paralysis, disease progression was attenuated [
15]. Cytokines like IL-17A and IL-17F, as well as IL-22 (a member of the IL-10 family) are produced by Th17 and evoke inflammation largely by stimulating fibroblasts, endothelial cells, epithelial cells and macrophages to produce chemokines, cytokines and matrix metalloproteinases (MMP), with the subsequent recruitment of polymorphonuclear leukocytes to sites of inflammation [
16]. In addition, Th17 cells have been associated with effective tumor immunity in a model of adoptive transfer of TCR transgenic CD4+ T cells specific for the shared self-tumor antigen tyrosinase-related protein 1 (TRP1) [
17]. These cells were used for the treatment of the poorly immunogenic B16 murine melanoma, and the therapeutic efficacy of Th1, Th17, and Th0 CD4+ T cell subsets was studied. The investigators demonstrated that the tumor-eradicating population was the Th17 cells [
17].
Tremelimumab is a fully human IgG2 monoclonal antibody with high binding affinity for human CTLA-4 [
18]. This antibody is in late stages of clinical development in patients with metastatic melanoma [
3,
4,
19]. It has a long plasma half life of 22 days, which is identical to the half life of endogenous IgG2s. When administered at doses of 10 to 15 mg/kg, plasma levels of tremelimumab beyond 30 μg/ml are achievable for 1 to 3 months [
19]. This sustained antibody concentration in plasma correlates with the
in vitro concentrations required to have a biological effect of CTLA4 blockade [
18], suggesting that sustained therapeutic levels of this antibody can be achieved with the doses administered to patients. The remarkably durable antitumor activity of tremelimumab in a small subset of patients is mediated by T cell-induced tumor regressions [
20], but its use is limited by autoimmune and inflammatory toxicities [
3,
4]. Therefore, understanding the mechanisms that lead to toxicity and antitumor response are of great importance to the development of CTLA4 blocking antibodies. Here we report the increase in Th17 cells in patients with metastatic melanoma after treatment with tremelimumab with or without DC vaccines, and its preferential increase in patients that develop clinically-relevant inflammatory and autoimmune toxicities.
Patients and methods
Description of Clinical Trials
Peripheral blood samples were obtained from leukapheresis procedures from 27 patients with metastatic melanoma that had been treated at UCLA in two investigator-initiated research protocols that included the anti-CTLA4 blocking antibody tremelimumab (Pfizer, New London, CT). In both clinical trials, patients underwent pre- and post-dosing apheresis collecting PBMC and plasma, and the UCLA IRB approved informed consent forms described their banking for immune monitoring assays. Six patients were treated in a phase I clinical trial of three biweekly intradermal (i.d.) administrations (study days 1, 14 and 28) of a fixed dose of 1 × 10
7 autologous DC pulsed with the MART-1
26–35 immunodominant peptide epitope (MART-1
26–35/DC) manufactured as previously described [
21], concomitantly with a dose escalation of tremelimumab at 10 (3 patients) and 15 mg/kg (3 other patients) every 3 months (UCLA IRB# 03-12-023, IND# 11579, Trial Registration number NCT0090896). The samples from these patients were coded with the study denomination of NRA and a patient-specific number. The remaining 21 patients were enrolled in a phase II clinical trial of single agent tremelimumab (UCLA IRB# 06-06-093, IND# 100453, Trial Registration number NCT00471887) administered at 15 mg/kg every 3 months. The samples from these patients were coded with the study denomination of GA and a patient-specific number. Objective clinical responses were recorded following a slightly modified Response Evaluation Criteria in Solid Tumors (RECIST) [
22]. The modification was to consider measurable disease lesions in the skin and subcutaneous lesions detectable by physical exam, but not by imaging exams, if they were adequately recorded at baseline using a camera with a measuring tape or ruler. Toxicities were recorded during the first 3 months of therapy (one cycle of tremelimumab-based therapy), since the post-dosing leukapheresis was performed only during the first cycle of therapy, most frequently between 30 and 60 days from the first dose of tremelimumab. The post-dosing leukapheresis were performed a median of 41 days after the dose of tremelimumab (range 28 to 81, with 6 cases out of the 30–60 day range). In all cases, concentrations of tremelimumab in peripheral blood should have been above 10 μg/ml at the time of cell harvesting by leukapheresis, which is the minimum concentration of tremelimumab that stimulated a biological effect consistent with CTLA4 blockade in preclinical studies [
18]. Adverse events attributed to tremelimumab by the study investigators were graded according to the NCI common toxicity criteria version 2.0 [
23]. Dose limiting toxicities (DLTs) were prospectively defined in both studies as any treatment-related toxicity equal or greater than grade 3, or the clinical evidence of grade 2 or higher autoimmune reaction in critical organs (heart, lung, kidney, bowel, bone marrow, musculoskeletal, central nervous system and the eye).
Sample Procurement and Processing
PBMC were collected from patients receiving tremelimumab-containing experimental immunotherapy by a leukapheresis procedure. Leukaphereses were planned as part of the pre-dosing procedures, and one to two months after receiving the first dose. Leukapheresis products were used to isolate PBMC by Ficoll-Hypaque (Amersham Pharmacia, Piscataway, New Jersey, USA) gradient centrifugation. PBMC were cryopreserved in liquid nitrogen in Roswell Park Memorial Institute medium (RPMI, Gibco-BRL, Gaithersburg, Maryland, USA) supplemented with 20% (all percentages represent v/v) heat-inactivated human AB serum (Omega Scientific, Tarzana, California, USA) and 10% dimethylsulfoxide (Sigma, St. Louis, Missouri, USA). One hundred milliliters of plasma were collected during the same apheresis procedures and were frozen at -20°C in 1 to 10 ml single use aliquots. Plasma samples were thawed and used immediately to measure cytokines.
Cytokine Detection in Plasma
Plasma samples from patients enrolled in the GA study were assessed for 12 cytokines using a cytokine suspension array detection system. The cytokines quantified were IL-1β, IL-2, IL-4, IL-5, IL-6, IL-10, IL-12 (p70), IL-13, tumor necrosis factor alpha (TNF-α), IFN-γ, granulocyte colony-stimulating factor (G-CSF), monocyte chemoattractant protein 1 (MCP-1/MCAF) and Chemokine (C-C motif) ligand 5, CCL-5 (RANTES). The assay was done according to the manufacturer's instructions in 96-well plates (Millipore, Billerica, Massachusetts, USA). Samples were analyzed using the Bio-Plex suspension array system (Bio-Rad Laboratories, Hercules, California, USA) and the Bio-Plex manager software with 5PL curve fitting. In addition, IL-17, a cytokine not represented in the multiplex cytokine detection kit described above, was quantified in plasma using a commercially available ELISA according to the manufacturer's instructions (eBioscience, San Diego, California, USA). Cytokine concentrations were analyzed in neat (undiluted) samples. The ranges of detection were from 6.9 to 5000 pg/ml for IL-4, IL-5, IL-6, IL-10, IL-13, TNF-α, from 12.3 to 9000 pg/ml for INF-γ and MCP-1, from 4.1 to 3000 pg/ml for RANTES and from 3.9 to 500 pg/ml for IL-17.
Cytokine Detection in Culture Supernatants
Cryopreserved PBMC aliquots collected before and after administration of tremelimumab within the GA and NRA studies were thawed and immediately diluted with RPMI complete media consisting of 10% human AB serum and 1% penicillin, streptomycin, and amphotericin (Omega Scientific). Cells were washed and subjected to enzymatic treatment with DNAse (0.002%, Sigma) for 1 hour at 37°C. Cells were washed again, and an aliquot of each sample was sorted using CD4+ magnetic cell sorting beads following the manufacturer's instructions (Miltenyi Biotec Inc., Auburn, California, USA). 2 × 106 pre- and post-dosing PBMC, and the same number of magnetic colum-sorted CD4+ cells, were incubated for 4 days with 50 ng/ml of anti-CD3 (OKT3, Ortho-Biotech, Bridgewater, New Jersey, USA) and 1 μg/ml of anti-CD28 (BD Biosciences, San Diego, California, USA) in 6-well plates. Cells were spun down, and the supernatants were collected for IL-17 by ELISA assay. All samples were measured in duplicates.
Intracellular Flow Cytometry for IL-17
To enumerate Th17 cells by ICS, PBMC or sorted CD4+ cells were activated as described above for 4 days in anti-CD3 and anti-CD28, and then re-stimulated for 5 hours with 5 μg/μl PMA and 5 μg/μl ionomycin in the presence of 1 μl/ml of a protein transport inhibitor containing brefeldin A (GolgiPlug, BD Biosciences) in FACS tubes. Cells were then surface stained with phycoerythrin (PE) anti-human CD4 and peridinin-chlorophyll-protein complex (PerCP) anti-CD3 (BD Biosciences) at room temperature for 15 minutes, permeabilized and then stained intracellularly with APC anti-IL-17 according to the manufacturer's instructions (eBioscience). Isotype antibody controls were used to enable correct compensation and to confirm antibody specificity. Flow cytometry analysis was conducted using FACSCalibur (BD Biosciences), and the data was analyzed using FlowJo software (Tree Star, Inc., San Carlos, California, USA).
Statistical analysis
Statistically significant differences in the concentration or percentage of IL-17 cytokine and Th17 cells between pre- and post-treatment samples were analyzed using a two-sided Student's paired t test using the Prism package (GraphPad Software, Inc., San Diego, California, USA). For all statistical analysis, the p value was set at p < 0.05. There was no correction for multiple comparisons, and all statistical analysis should be considered exploratory. All error bars shown in this paper are standard errors of the means (SEM).
Discussion
Dose-escalation studies with CTLA4 blocking monoclonal antibodies provide clear evidence that increasing the antibody dose and exposure results in increasing toxicities consistent with breaking tolerance to self tissues, and at higher dosing levels, some patients benefit with durable tumor regressions [
4,
19,
24]. Understanding the mechanism of both phenomena is of critical importance for this class of agents. It seems highly unlikely that the lymphocytes that mediate melanoma antitumor responses are the same as the ones that mediate toxicities like colitis, hypophysitis or thyroiditis, since there is little evidence of shared antigen profiles recognized by effector T cells among these tissues. Therefore, many studies have focused on studying immune cell subsets that are implicated in maintenance of peripheral tolerance. In particular, a lot of effort has been focused on detecting if Treg are decreased or functionally impaired in patients receiving CTLA4 blocking monoclonal antibodies. The interest is based on several lines of evidence, including the overlapping phenotype of autoimmune conditions in CTLA4 and FoxP3 deficient mice, and evidence that Treg-specific deficiency in CTLA4 expression impairs the suppressive function of Tregs [
25]. The relatively high basal level of CTLA4 on Treg compared to activated T effector cells (which is the prime target for these blocking antibodies), and the clinical evidence of the modulation of peripheral tolerance with CTLA4 blocking antibodies, provided grounds for studying the implication of Treg in patient-derived samples. Most data reported to date demonstrate that the number of circulating cells with a Treg phenotype (CD4, CD25, FoxP3 positive) does not decrease after the administration of CTLA4 antibodies. In fact, there is a clear trend towards an increase in these cells [
26‐
29], a finding that is not that surprising taking into account that these antibodies are blocking but not depleting antibodies for CTLA4 positive cells. Also, the number of cells staining positive for FoxP3 by immunohistochemistry increases in tumor biopsies of regressing lesions after CTLA4 blockade [
20]. Data on functional modulation of Treg is not that clear, with mixed results on the detection of Treg-mediated suppression of effector T cells [
26,
28,
29].
An alternative possibility studied by us is that Th17 cells, an immune cell subset implicated in mediating autoimmunity and in chronic inflammatory conditions, may be modulated by CTLA4 blocking antibodies. There is a reciprocal negative correlation between Treg and Th17 mediated by IL-2 [
30], suggesting that their effects may be mutually exclusive as opposed to redundant. There is evidence that CTLA4 is expressed on murine Th17 cells at levels that are higher than Th1 cells [
31], while CTLA4 has also been demonstrated on human Th17 cells [
32]. Since both tremelimumab and ipilimumab, the two CTLA4 blocking antibodies in clinical development, inhibit CTLA4 negative signaling without inducing antibody-dependent cellular cytotoxicity (ADCC) [
18,
33], it is certainly possible that these antibodies would release negative signaling in Th17 resulting in increased number or function. In this study we analyzed IL-17 cytokine and cytokine-producing cells in peripheral blood of patients treated with tremelimumab with the goal of exploring if Th17 may be involved in the clinical events in patients receiving CTLA4 blocking monoclonal antibodies. Our data provides preliminary evidence that this may be the case. The modulation of Th17 levels is not large in magnitude, but is was highly reproducible among different assay conditions. Although we could not detect differences in IL-17 cytokine levels after dosing in plasma samples obtained directly from peripheral blood, the cells that had ability to produce IL-17 upon non-specific
ex vivo stimulation increased in post-dosing blood cell samples from patients. This could be detected by quantifying soluble cytokine in culture supernatants and by determining the number of cells with intracellular IL-17 by flow cytometry. In addition, the results were comparable when we analyzed cultures from whole PBMC (including many immune and non-immune cell subsets other than CD4 T helper cells) and with sorted populations containing CD4 cells alone.
Th17 may be implicated in toxicities as well as responses after administration of anti-CTLA4 antibodies. Besides the well recognized implication of Th17 in murine and human inflammatory and autoimmune conditions [
8], it is becoming clearer that they may also have a role in mediating antitumor immunity [
17]. Therefore, we explored if the increases in Th17 cells were more prominent in the subsets of patients with toxicity or tumor responses. Although we found no correlation between IL-17 production and responses to therapy, our exploratory analysis suggests that the post-dosing increase in the levels of IL-17 in culture supernatants and by intracellular flow cytometry were higher in the small number of patients with toxicity. For this analysis, we restricted to clinically-significant toxicities that followed the prospective definition of DLTs in the clinical trial protocols, and which happened during the first cycle of therapy, the closest time to the obtaining of post-dosing samples in these patients. When samples from these patients were analyzed separately from samples from patients with lower levels of toxicity or no toxicities, differences between pre- and post-dosing samples were only evident in samples from patients with DLTs. The significance of increases in Th17 disappeared from the group of patients with non-DLT toxicities. Of note, patients with the highest levels of Th17 cells were not the ones who developed toxicities, suggesting to us that it is a doubling of the number of Th17 after tremelimumab may be linked to toxicities as opposed to the absolute number at any given time point. Our exploratory analysis is obviously limited by the small number of patients in this series, and will need to be confirmed in larger groups. However, the findings are reproducible in all of the different experimental conditions used to analyze IL-17-producing cells, which provides confidence in these results. From this work we conclude that Th17 may be implicated in the clinical effects of CTLA4 blocking monoclonal antibodies, and further study of their role in treatment-induced toxicities may help in elucidating how toxicities and responses may be differentially modulated with this mode of therapy.
Acknowledgements
EvE was supported by grants from the Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), and the Fundación Sales, Buenos Aires, Argentina. AR was supported by the Harry J. Lloyd Charitable Trust, P50 CA086306, U54 CA119347 and RN2-00902-1 New Faculty Award 2 from the California Institute for Regenerative Medicine (CIRM). Flow cytometry assays were performed in the UCLA Jonsson Comprehensive Cancer Center (JCCC) and Center for AIDS Research Flow Cytometry Core Facility that is supported by National Institutes of Health awards CA-16042 and AI-28697 and by the JCCC, the UCLA AIDS Institute, and the David Geffen School of Medicine at UCLA. Patients were treated at the UCLA General Clinical Research Center (G-CRC), which is supported by USPHS Grant M01-RR-0865.
Competing interests
AR has received research funding and honoraria from Pfizer. The other authors have no competing interests on this work.
Authors' contributions
EVE and AR conceived and designed the study. EVE, TC and NA carried out the experiments. JJ and BC-A provided the human samples for analysis. RCK and BC-A contributed to the assay conduct and data interpretation. EVE and AR wrote the manuscript. All authors read and approved the final manuscript.